FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P080011
·
Supplement: S047
·
Decision Oct 11, 2016
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- BIOFINITY XR TORIC
- PMA Number
- P080011
- Supplement Number
- S047
- Device Class
- FDA Class 3
- Product Code
- LPM
- Generic Name
- Lenses, soft contact, extended wear
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 11, 2016
- Date Received
- September 19, 2016
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Installation and validation of Biofinity MTO production Line 1, collation and packaging module, at the CooperVision, Inc. Hamble, UK manufacturing facility to support post autoclave processing of Biofinity XR Toric.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LPM | Lenses, Soft Contact, Extended Wear | FDA class 3 | Ophthalmic |